- Rush University Medical Center (Chicago, IL)
- …Assistant is responsible for collecting information according to the research study protocols. The Research Assistant conducts assessments and collect data and/or ... biological samples from research studies . In addition, the Research Assistant assists in writing...settings. * May require 6-8 weeks training depending on study protocols. * Availability to work evenings, overnight and… more
- Rush University Medical Center (Chicago, IL)
- …and collect data and/or biological samples from research participants and families in studies . Exemplifies the Rush mission, vision and values and acts in accordance ... settings. * May require 6-8 weeks training depending on study protocols. * Availability to work evenings, overnight and...evenings, overnight and weekends if called for under the study protocols. * May require personal transportation to field… more
- Tufts Medicine (Boston, MA)
- …will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. This role sits in Neurology and is patient facing. ... may be assigned. 1. Assists in the recruitment of study participants. 2. Completes follow up with study... study participants. 2. Completes follow up with study participants in prescribed settings as required. 3. Completes… more
- Sanford Health (Fargo, ND)
- …nursing practice with the opportunity to contribute to meaningful clinical studies , helping to improve treatments and outcomes for pediatric patients and ... the research process. Advanced nursing position that involves clinical patient contact, research study coordination and study data management. Must be able to… more
- Lilly (Indianapolis, IN)
- …as mandated by corporate patient safety; the review process for protocols, study reports, publications and data dissemination for products, new and updated labels, ... realization. The CRP serves as a scientific resource for study teams, departments, and others as needed. The Clinical...personnel. + Monitor patient safety during the conduct of studies and conduct the appropriate tracking and follow-up of… more
- Stanford University (Stanford, CA)
- …clinical staff, researchers, outside vendors, and other staff to administer treatment and study protocols. May coordinate multi-site studies . + Conduct study ... Responsibilities include providing clinical and administrative nursing support, administering study medications and evaluating participants for adverse events. The… more
- University of Washington (Seattle, WA)
- …(30%)** + Implement and maintain subject recruitment protocols. + Communicate with potential study families to explain the study , answer questions, and solve ... problems. + Administer screening questions to determine eligibility and recruit into study . + Implement and maintain tracking protocols in general. + Implement and… more
- Johns Hopkins University (Baltimore, MD)
- …to the IRB. + With guidance, prepares other forms required for study initiation (pre-printed orders, eligibility checklists, etc.) + Determines that IRB approval ... prior to initiation of research activity. + Participates in study initiation meetings. + Prepares space for study...& ongoing eligibility of all subjects for assigned research studies . + Screens potential research subjects for participation in… more
- Johns Hopkins University (Baltimore, MD)
- Researchers at Johns Hopkins University conduct clinical trials and clinical studies to discover new ways to prevent and treat diseases and other health problems. We ... will administratively coordinate clinical protocol implementation, typically for a single study . Will ensure the efficient logistical implementation of the study… more
- IQVIA (Parsippany, NJ)
- …Practice (GCP), local regulatory requirements, etc. + Develop and document the study -specific training plan for assigned studies . + Conduct and/or supports ... **Job Summary:** CTL&D Analyst provides support to CTL&D for study -specific training planning within various therapeutic area(s). Service/deliverables include… more
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